Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:57185984-57186342 | Common:1; Rare:104 | ||||
chr16:57447354-57447511 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
chr16:58129268-58129581 | Common:4; Rare:101 | ||||
chr16:58629786-58630032 | Common:1; Rare:66 | ||||
chr16:58734234-58734436 | Common:4; Rare:61 | ||||
chr16:65122019-65122192 | Common:1; Rare:59 | ||||
chr16:66552499-66552654 | Rare:67 | ||||
chr16:66934353-66934506 | Common:1; Rare:57 | ||||
chr16:67226859-67227163 | Common:1; Rare:108 | ||||
chr16:67481126-67481331 | Common:1; Rare:71 | ||||
chr16:67528701-67528861 | Rare:45 | ||||
chr16:67846700-67846975 | Common:1; Rare:74 | ||||
chr16:68023209-68023296 | Common:1; Rare:22 | ||||
chr16:68264367-68264558 | Rare:58 | ||||
chr16:68310922-68311062 | Common:1; Rare:67 |